Holly A, Sittinger M, Bujia J
Department of Otorhinolaryngology, Ludwig-Maximilians University, Klinikum Grosshadern, Munich, Germany.
Eur Arch Otorhinolaryngol. 1995;252(6):366-9. doi: 10.1007/BF00178279.
Cholesteatoma epithelium is characterized by a dysregulation with a hyperproliferative growth and altered differentiation. In a variety of cells c-myc oncogene was found to be highly linked to the control of growth and differentiation. Expression of c-myc was studied in cholesteatoma epithelium using a monoclonal antibody directed against the 67 kDa c-myc protein product and the alkaline phosphatase-antialkaline phosphatase method. For quantitative analysis a computer-linked analyzing system was used. In contrast to normal skin, keratinocytes of basal and suprabasal layers showed nuclear staining in cholesteatoma epithelium. The extent of nuclear staining of epithelial cells in the cholesteatomas studied was significantly increased. Concurrent cytoplasmic staining was observed in both skin and cholesteatoma, but with a stronger reactivity in the latter. These findings suggest participation of the c-myc oncogene in cholesteatoma epithelium.
胆脂瘤上皮的特征是生长失调,具有过度增殖性生长和分化改变。在多种细胞中,发现c-myc癌基因与生长和分化的控制高度相关。使用针对67 kDa c-myc蛋白产物的单克隆抗体和碱性磷酸酶-抗碱性磷酸酶方法,研究了胆脂瘤上皮中c-myc的表达。为进行定量分析,使用了计算机连接分析系统。与正常皮肤相比,胆脂瘤上皮中基底层和基底上层的角质形成细胞显示出核染色。在所研究的胆脂瘤中,上皮细胞核染色程度显著增加。在皮肤和胆脂瘤中均观察到同时存在的细胞质染色,但在后者中反应性更强。这些发现提示c-myc癌基因参与了胆脂瘤上皮形成。